Identity
- Trade Name
- LF900 FDA UDI
- Generic Name
- Sequential venous compression system inflator FDA UDI
- Device Name
- Main device 1ea, OVERLAPPING HALF LEG SLEEVE Medium Wide(MW403) 2ea, Double Hose 1ea [One set box] FDA UDI
- Model / Reference
- LF90100-OHW FDA UDI
- Description
- Main device 1ea, OVERLAPPING HALF LEG SLEEVE Medium Wide(MW403) 2ea, Double Hose 1ea [One set box] FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809802644618 FDA UDI
- 510(k) Number
- K231437 FDA UDI
- FDA Product Code
- IRP FDA UDI
- GMDN Term
- Sequential venous compression system inflator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5650 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Sequential venous compression system inflator
Lf900 by Daesung Maref Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Sequential venous compression system inflator.
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- Air Relax Classic Model AR-2.0 Leg Recovery System - Size 2 — Maxstar Industrial Co., Ltd. · Class II
- TRIPLE PLAY — Compression Solutions, LLC · Class II
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- Wright — Wright Therapy Products, Inc. · Class II
Cleared under the same submission
K231437 also covers:
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
- LF900 — DAESUNG MAREF CO., LTD.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Daesung Maref Co., Ltd.
Sources (1)
- FDA UDI 4859a2f1-39eb-4bb8-b72b-4c3912979372 34 fields · synced Jun 1, 2026